MA53352A - Dérivés de pyridin-2-(1h)-one-quinolinone en tant qu'inhibiteurs d'isocitrate déshydrogénase - Google Patents

Dérivés de pyridin-2-(1h)-one-quinolinone en tant qu'inhibiteurs d'isocitrate déshydrogénase

Info

Publication number
MA53352A
MA53352A MA053352A MA53352A MA53352A MA 53352 A MA53352 A MA 53352A MA 053352 A MA053352 A MA 053352A MA 53352 A MA53352 A MA 53352A MA 53352 A MA53352 A MA 53352A
Authority
MA
Morocco
Prior art keywords
pyridin
isocitrate dehydrogenase
dehydrogenase inhibitors
quinolinone derivatives
quinolinone
Prior art date
Application number
MA053352A
Other languages
English (en)
Inventor
Susan Ashwell
Ann-Marie Campbell
Justin Andrew Caravella
R Bruce Diebold
Anna Ericsson
Gary Gustafson
David R Lancia Jr
Jian Lin
Wei Lu
Zhongguo Wang
Original Assignee
Forma Therapeutics Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Forma Therapeutics Inc filed Critical Forma Therapeutics Inc
Publication of MA53352A publication Critical patent/MA53352A/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
MA053352A 2014-09-19 2015-09-18 Dérivés de pyridin-2-(1h)-one-quinolinone en tant qu'inhibiteurs d'isocitrate déshydrogénase MA53352A (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201462053006P 2014-09-19 2014-09-19
US201562128089P 2015-03-04 2015-03-04
US201562150812P 2015-04-21 2015-04-21

Publications (1)

Publication Number Publication Date
MA53352A true MA53352A (fr) 2021-09-15

Family

ID=54291606

Family Applications (2)

Application Number Title Priority Date Filing Date
MA040481A MA40481A (fr) 2014-09-19 2015-09-18 Dérivés de pyridin-2-(1h)-one-quinolinone à titre d'inhibiteurs d'isocitrate déshydrogénase mutante
MA053352A MA53352A (fr) 2014-09-19 2015-09-18 Dérivés de pyridin-2-(1h)-one-quinolinone en tant qu'inhibiteurs d'isocitrate déshydrogénase

Family Applications Before (1)

Application Number Title Priority Date Filing Date
MA040481A MA40481A (fr) 2014-09-19 2015-09-18 Dérivés de pyridin-2-(1h)-one-quinolinone à titre d'inhibiteurs d'isocitrate déshydrogénase mutante

Country Status (36)

Country Link
US (8) US9834539B2 (fr)
EP (4) EP4257131A3 (fr)
JP (1) JP6648115B2 (fr)
KR (1) KR102209667B1 (fr)
CN (3) CN117695280A (fr)
AU (3) AU2015317329B2 (fr)
BR (1) BR112017005238B1 (fr)
CA (1) CA2961817C (fr)
CL (1) CL2017000658A1 (fr)
CO (1) CO2017003241A2 (fr)
CY (2) CY1121149T1 (fr)
DK (2) DK3447050T3 (fr)
EA (1) EA034336B1 (fr)
EC (1) ECSP17022933A (fr)
ES (3) ES2953347T3 (fr)
FI (1) FI3733662T3 (fr)
HR (1) HRP20200666T1 (fr)
HU (2) HUE062424T2 (fr)
IL (3) IL292608A (fr)
LT (2) LT3194376T (fr)
MA (2) MA40481A (fr)
ME (1) ME03776B (fr)
MX (2) MX2017003404A (fr)
MY (2) MY176250A (fr)
NZ (2) NZ730373A (fr)
PE (1) PE20171056A1 (fr)
PH (1) PH12017500517A1 (fr)
PL (3) PL3194376T3 (fr)
PT (3) PT3194376T (fr)
RS (2) RS60140B1 (fr)
SA (1) SA517381129B1 (fr)
SG (1) SG11201702194SA (fr)
SI (2) SI3194376T1 (fr)
TW (1) TWI686390B (fr)
WO (1) WO2016044789A1 (fr)
ZA (2) ZA201702127B (fr)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102985557B (zh) 2009-03-13 2018-06-15 安吉奥斯医药品有限公司 用于细胞增殖相关病症的方法和组合物
EP2491145B1 (fr) * 2009-10-21 2016-03-09 Agios Pharmaceuticals, Inc. Procédés et compositions pour des troubles relatifs à la prolifération cellulaire
EP3406609A1 (fr) 2014-02-06 2018-11-28 Heptares Therapeutics Limited Composés aza bicycliques en tant qu'agonistes du récepteur muscarinique
AU2015317321B2 (en) * 2014-09-19 2020-03-12 Forma Therapeutics, Inc. Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors
CA2961807A1 (fr) 2014-09-19 2016-03-24 Forma Therapeutics, Inc. Derives de phenylquinoleinone en tant qu'inhibiteurs d'isocitrate deshydrogenase mutante
ES2953347T3 (es) 2014-09-19 2023-11-10 Forma Therapeutics Inc Derivados de piridin-2(1H)-ona quinolinona como inhibidores de isocitrato deshidrogenasa mutante
MA39484A (fr) 2014-09-19 2016-03-24 Bayer Pharma AG Indazoles à substituants benzyle utilisés comme inhibiteurs de bub1
MX2017003626A (es) 2014-09-19 2018-01-24 Forma Therapeutics Inc Derivados de piridinil quinolinona como inhibidores de isocitrato deshidrogenasa mutante (mt-idh).
ES2905564T3 (es) * 2014-12-22 2022-04-11 Us Health Inhibidores mutantes de IDH1 útiles para tratar el cáncer
WO2016171755A1 (fr) 2015-04-21 2016-10-27 Forma Therapeutics, Inc. Dérivés de phénylquinoléinone en tant qu'inhibiteurs de l'isocitrate déshydrogénase mutante
WO2016171756A1 (fr) 2015-04-21 2016-10-27 Forma Therapeutics, Inc. Composés hétérocycliques de quinoléinone à cinq chaînons comme inhibiteurs de l'isocitrate déshydrogénase mutante
PL3619196T3 (pl) 2017-05-04 2022-08-29 Bayer Cropscience Aktiengesellschaft Pochodne 2-{[2-(fenyloksymetylo)pirydyn-5-yl]oksy}-etanoaminy i związki pokrewne jako środki do zwalczania szkodników np. do ochrony upraw
US20210196701A1 (en) 2018-05-16 2021-07-01 Forma Therapeutics, Inc. Inhibiting mutant idh-1
PL3720442T3 (pl) 2018-05-16 2023-05-29 Forma Therapeutics, Inc. Hamowanie mutanta idh-1
US11013734B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation
US10532047B2 (en) 2018-05-16 2020-01-14 Forma Therapeutics, Inc. Solid forms of ((S)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile
US11311527B2 (en) 2018-05-16 2022-04-26 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1)
WO2020232381A1 (fr) 2019-05-16 2020-11-19 Forma Therapeutics, Inc. Inhibition de l'isocitrate déshydrogénase 1 mutante (midh-1)
US11013733B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1)
TW202104207A (zh) * 2019-04-17 2021-02-01 美商健生生物科技公司 二氫乳清酸脫氫酶抑制劑
US11566013B1 (en) * 2019-11-20 2023-01-31 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH1)
CN112321571B (zh) * 2020-10-27 2022-06-03 浙江工业大学 2-呋喃-喹啉-4-甲酰胺类化合物及其应用
CN112341389B (zh) * 2020-10-27 2022-07-29 浙江工业大学 一种含氮芳杂环取代的喹啉甲酰胺类衍生物及其应用
CN115850240B (zh) * 2022-12-28 2023-09-19 北京康立生医药技术开发有限公司 一种治疗急性髓系白血病药物奥卢他西尼的合成方法

Family Cites Families (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL99731A0 (en) 1990-10-18 1992-08-18 Merck & Co Inc Hydroxylated pyridine derivatives,their preparation and pharmaceutical compositions containing them
US5262564A (en) 1992-10-30 1993-11-16 Octamer, Inc. Sulfinic acid adducts of organo nitroso compounds useful as retroviral inactivating agents anti-retroviral agents and anti-tumor agents
US20030105124A1 (en) 2000-04-27 2003-06-05 Susan Beth Sobolov-Jaynes Substituted benzolactam compounds
EP1534703A2 (fr) 2002-06-12 2005-06-01 Abbott Laboratories Antagonistes du recepteur de l'hormone de melano-concentration
WO2004043936A1 (fr) 2002-11-14 2004-05-27 Kyowa Hakko Kogyo Co., Ltd. Inhibiteurs de plk (kinases du type polo)
RU2284325C2 (ru) 2003-12-17 2006-09-27 Общество С Ограниченной Ответственностью "Асинэкс Медхим" Производные фенил-3-аминометил-хинолона-2 в качестве ингибиторов no-синтетазы, способ их получения, биологически активные соединения и фармацевтическая композиция на их основе
US7956060B2 (en) 2004-03-30 2011-06-07 Kyowa Hakko Kirin Co., Ltd. Pyrimidine derivative compound
WO2006054912A1 (fr) * 2004-11-18 2006-05-26 Obchestvo S Ogranichennoy Otvetstvennost'u 'asineks Medhim' Derives d'aryl(hetaryl)-3-aminomethylchinolone-2 utilises en tant qu'inhibiteurs de no-synthetase et de cyclo-oxygenase-2, procedes de leur fabrication et compositions pharmaceutiques sur leur base
TW200803855A (en) 2006-02-24 2008-01-16 Kalypsys Inc Quinolones useful as inducible nitric oxide synthase inhibitors
CA2657287A1 (fr) * 2006-07-17 2008-01-24 Merck & Co., Inc. Composes de 1-hydroxy naphtyridine en tant qu'agents anti-vih
JP2010043004A (ja) 2006-12-06 2010-02-25 Dainippon Sumitomo Pharma Co Ltd 新規2環性複素環化合物
JP5450381B2 (ja) 2007-04-30 2014-03-26 プロメティック・バイオサイエンスィズ・インコーポレーテッド 化合物、そのような化合物を含有する組成物、及びそのような化合物を用いるがん及び自己免疫疾患の治療法
JP2012529511A (ja) 2009-06-08 2012-11-22 アブラクシス バイオサイエンス リミテッド ライアビリティー カンパニー トリアジン誘導体類及びそれらの治療応用
WO2011072174A1 (fr) * 2009-12-09 2011-06-16 Agios Pharmaceuticals, Inc. Composés thérapeutiquement actifs destinés au traitement d'un cancer caractérisé par une mutation idh
WO2012006104A2 (fr) 2010-06-28 2012-01-12 Academia Sinica, Taiwan Composés et procédés destinés au traitement d'une infection par la tuberculose
CN102558049B (zh) * 2010-12-17 2015-02-04 中国科学院上海药物研究所 一类双香豆素类化合物及其制备方法和用途
US20120184562A1 (en) 2011-01-19 2012-07-19 Kin-Chun Luk 1,6- and 1,8-naphthyridines
US20120184548A1 (en) 2011-01-19 2012-07-19 Romyr Dominique Carboxylic acid aryl amides
WO2012129562A2 (fr) 2011-03-24 2012-09-27 The Scripps Research Institute Composés et procédés pour l'induction de la chondrogenèse
CN102827170A (zh) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 治疗活性组合物和它们的使用方法
CN103814020B (zh) * 2011-06-17 2017-07-14 安吉奥斯医药品有限公司 治疗活性组合物和它们的使用方法
CA2849995A1 (fr) 2011-09-27 2013-04-04 Novartis Ag 3-pyrimidin-4-yl-oxazolidin-2-ones comme inhibiteurs d'idh mutante
CN104271132B (zh) 2011-12-21 2018-01-12 科罗拉多大学董事会法人团体 靶向Ral GTP酶的抗癌化合物及使用其的方法
MX358940B (es) 2012-01-06 2018-09-10 Agios Pharmaceuticals Inc Star Compuestos terapéuticamente activos y sus métodos de uso.
BR112015022483A2 (pt) * 2013-03-14 2017-07-18 Novartis Ag 3-pirimidin-4-il-oxazolidin-2-onas como inibidores de idh mutante
US10478445B2 (en) 2013-07-03 2019-11-19 Georgetown University Boronic acid derivatives of resveratrol for activating deacetylase enzymes
CA2939026A1 (fr) 2014-02-11 2015-08-20 Bayer Pharma Aktiengesellschaft Benzimidazol-2-amines en tant qu'inhibiteurs midh1
AU2015317321B2 (en) 2014-09-19 2020-03-12 Forma Therapeutics, Inc. Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors
CA2961807A1 (fr) 2014-09-19 2016-03-24 Forma Therapeutics, Inc. Derives de phenylquinoleinone en tant qu'inhibiteurs d'isocitrate deshydrogenase mutante
MX2017003626A (es) 2014-09-19 2018-01-24 Forma Therapeutics Inc Derivados de piridinil quinolinona como inhibidores de isocitrato deshidrogenasa mutante (mt-idh).
ES2953347T3 (es) 2014-09-19 2023-11-10 Forma Therapeutics Inc Derivados de piridin-2(1H)-ona quinolinona como inhibidores de isocitrato deshidrogenasa mutante
ES2905564T3 (es) 2014-12-22 2022-04-11 Us Health Inhibidores mutantes de IDH1 útiles para tratar el cáncer
GB2533925A (en) 2014-12-31 2016-07-13 Univ Bath Antimicrobial compounds, compositions and methods
WO2016171756A1 (fr) 2015-04-21 2016-10-27 Forma Therapeutics, Inc. Composés hétérocycliques de quinoléinone à cinq chaînons comme inhibiteurs de l'isocitrate déshydrogénase mutante
WO2016171755A1 (fr) 2015-04-21 2016-10-27 Forma Therapeutics, Inc. Dérivés de phénylquinoléinone en tant qu'inhibiteurs de l'isocitrate déshydrogénase mutante
WO2017019429A1 (fr) 2015-07-27 2017-02-02 Eli Lilly And Company Coposés de 7-phényléthylamino -4 h-pyrimido [4,5-d] [1,3] oxazin-2-one et leur utilisation en tant qu'inhibiteurs de idh1 mutante
MX2018010261A (es) 2016-02-26 2019-02-11 Agios Pharmaceuticals Inc Inhibidores de idh1 para el tratamiento de neoplasias malignas hematologicas y tumores solidos.
US10696665B2 (en) 2016-06-06 2020-06-30 Eli Lilly And Company Mutant IDH1 inhibitors
CN109641887B (zh) 2016-06-22 2022-09-20 美国政府健康及人类服务部 可用作用于治疗癌症的突变idh1抑制剂的噻唑衍生物
NZ754115A (en) 2016-12-16 2021-07-30 Lilly Co Eli 7-phenylethylamino-4h-pyrimido[4,5-d][1,3]oxazin-2-one compounds as mutant idh1 and idh2 inhibitors

Also Published As

Publication number Publication date
HRP20200666T1 (hr) 2020-07-24
IL282363A (en) 2021-06-30
PL3447050T3 (pl) 2020-07-27
BR112017005238A2 (pt) 2017-12-19
US10550098B2 (en) 2020-02-04
PL3733662T3 (pl) 2024-01-22
EP3733662B1 (fr) 2023-06-07
PT3194376T (pt) 2019-02-04
RS60140B1 (sr) 2020-05-29
CN107001328A (zh) 2017-08-01
TWI686390B (zh) 2020-03-01
CA2961817A1 (fr) 2016-03-24
MA40481A (fr) 2017-07-26
AU2019283765A1 (en) 2020-01-16
KR102209667B1 (ko) 2021-01-29
MY197533A (en) 2023-06-21
ZA201702127B (en) 2019-06-26
US20210078973A1 (en) 2021-03-18
ES2953347T3 (es) 2023-11-10
ES2790640T3 (es) 2020-10-28
AU2019283765B2 (en) 2021-05-13
US20170174658A1 (en) 2017-06-22
CN117695280A (zh) 2024-03-15
LT3194376T (lt) 2019-02-25
US20180312487A1 (en) 2018-11-01
AU2015317329A1 (en) 2017-04-27
ES2704897T3 (es) 2019-03-20
PE20171056A1 (es) 2017-07-21
JP2017528487A (ja) 2017-09-28
PT3447050T (pt) 2020-09-17
AU2015317329B2 (en) 2019-10-31
CN111909130A (zh) 2020-11-10
EP4257131A2 (fr) 2023-10-11
HUE041460T2 (hu) 2019-05-28
CN107001328B (zh) 2020-06-05
AU2021215141B2 (en) 2023-10-19
WO2016044789A1 (fr) 2016-03-24
AU2021215141A1 (en) 2021-09-02
PT3733662T (pt) 2023-08-18
NZ730373A (en) 2019-11-29
BR112017005238B1 (pt) 2023-01-17
US20190263778A1 (en) 2019-08-29
MY176250A (en) 2020-07-24
IL251163A0 (en) 2017-04-30
MX2019013203A (es) 2020-01-20
SI3194376T1 (sl) 2019-03-29
US10889567B2 (en) 2021-01-12
ECSP17022933A (es) 2017-08-31
US10414752B2 (en) 2019-09-17
EA034336B1 (ru) 2020-01-29
EP3447050A1 (fr) 2019-02-27
CA2961817C (fr) 2024-03-12
EP4257131A3 (fr) 2024-01-10
CO2017003241A2 (es) 2017-09-20
DK3194376T3 (en) 2019-01-21
CN111909130B (zh) 2023-10-31
US9834539B2 (en) 2017-12-05
FI3733662T3 (fi) 2023-08-09
SA517381129B1 (ar) 2021-04-26
MX2017003404A (es) 2017-07-28
CL2017000658A1 (es) 2017-12-22
EP3447050B1 (fr) 2020-02-19
RS58184B1 (sr) 2019-03-29
HUE062424T2 (hu) 2023-11-28
US20230125739A1 (en) 2023-04-27
ZA201902446B (en) 2023-12-20
EP3194376B1 (fr) 2018-10-24
US11498913B2 (en) 2022-11-15
PL3194376T3 (pl) 2019-05-31
IL251163B (en) 2021-05-31
PH12017500517A1 (en) 2017-08-07
NZ758641A (en) 2023-12-22
CY1122865T1 (el) 2021-05-05
EP3733662A1 (fr) 2020-11-04
LT3447050T (lt) 2020-05-11
IL292608A (en) 2022-07-01
DK3447050T3 (da) 2020-03-09
EP3194376A1 (fr) 2017-07-26
KR20170063742A (ko) 2017-06-08
ME03776B (fr) 2021-04-20
US20160083366A1 (en) 2016-03-24
IL282363B (en) 2022-06-01
EA201790657A8 (ru) 2018-02-28
JP6648115B2 (ja) 2020-02-14
EA201790657A1 (ru) 2017-08-31
SI3447050T1 (sl) 2020-08-31
US20240150319A1 (en) 2024-05-09
SG11201702194SA (en) 2017-04-27
CY1121149T1 (el) 2020-05-29
US20200223822A1 (en) 2020-07-16
TW201617335A (zh) 2016-05-16

Similar Documents

Publication Publication Date Title
MA53352A (fr) Dérivés de pyridin-2-(1h)-one-quinolinone en tant qu'inhibiteurs d'isocitrate déshydrogénase
MA47123A (fr) Dérivés de benzooxazole en tant qu'mmunomodulateurs
MA47125A (fr) Dérivés de pyrazole en tant qu'inhibiteurs de malt1
MA40774A (fr) Dérivés de diaryle-urée en tant qu'inhibiteurs de kinase p38
MA45189A (fr) Nouveaux dérivés hétérocycliques utiles en tant qu'inhibiteurs de shp2
MA45244A (fr) Pyridines substituées utilisées en tant qu'inhibiteurs de dnmt1
MA55194A (fr) Composés hétérocycliques en tant qu'immunomodulateurs
MA51878A (fr) Composés d'aminothiazole en tant qu'inhibiteurs de c-kit
CL2016002736A1 (es) Inhibidores de demetilasa-1 específico de lisina
MA40587A (fr) Composés d'aminopyrimidinyle en tant qu'inhibiteurs de jak
MA46981A (fr) Dérivés de benzimidazole en tant qu'inhibiteurs de bromodomaine
MA40943A (fr) Pyrrolopyridines substituées utilisées en tant qu'inhibiteurs de bromodomaines
MA40940A (fr) Pyrrolopyridines substituées utilisées en tant qu'inhibiteurs de bromodomaines
MA41140A (fr) Dérivés de 2,4-dioxo-quinazoline-6-sulfonamide en tant qu'inhibiteurs de la parg
MA54253A (fr) Procédé de préparation de dérivés de 2-chloro-4-hétéroaryl-pyridimidines
MA54567A (fr) Pyridine et composés de pyridimine en tant qu'inhibiteurs de pi3k-gamma
DK3286177T3 (da) Quinolinderivater som tam rtk-inhibitorer
MA46878A (fr) Composés de benzodiazolium en tant qu'inhibiteurs d'enac
DK3261726T3 (da) Sammensætning til behandling af acne
IL250038A0 (en) 4,5 - dehydroisoxazole derivatives used as nampt inhibitors
DK3202766T3 (da) Isoxazolderivat som muteret isocitratdehydrogenase 1-inhibitor
HK1253572A1 (zh) 作為tnap抑制劑的吡啶並噁嗪酮化合物
DK3216451T3 (da) Oftalmisk vandig sammensætning
FR3023290B1 (fr) Derives de flavaglines
MA41174A (fr) Dérivés d'imidazopyridazine utilisés en tant qu'inhibiteurs de pi3kbeta